Mowat–Wilson syndrome in a Chinese population: A case series
Author:
Affiliation:
1. Clinical Genetic ServiceDepartment of Health, HKSAR Hong Kong
2. Department of Paediatrics and Adolescent Medicine, Li Ka Shing Faculty of MedicineThe University of Hong Kong Hong Kong
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.61557
Reference16 articles.
1. Clinical features and management issues in Mowat–Wilson syndrome
2. Large-Scale Deletions and SMADIP1 Truncating Mutations in Syndromic Hirschsprung Disease with Involvement of Midline Structures
3. Recurrence of Mowat-Wilson syndrome in siblings with a novel mutation in theZEB2gene
4. Mowat-Wilson syndrome: Facial phenotype changing with age: Study of 19 Italian patients and review of the literature
5. ZEB2 zinc-finger missense mutations lead to hypomorphic alleles and a mild Mowat–Wilson syndrome
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3. Unilateral progressive anterior iris adhesions in Mowat-Wilson syndrome: a new ocular finding;Journal of American Association for Pediatric Ophthalmology and Strabismus;2024-02
4. Clinical Characteristics and Novel ZEB2 Gene Mutation Analysis of Three Chinese Patients with Mowat-Wilson Syndrome;Pharmacogenomics and Personalized Medicine;2023-08
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